Drug Safety Advisor

Job content

This job is located in Zaventem (Belgium) – please apply only if you live in Belgium.

Qplus consult offers high-level quality services for pharmaceutical companies. Within the pharmaceutical sector Qplus consult built a solid and strong reputation, therefore we are looking for a motivated, dynamic and flexible Drug Safety Advisor to join our team.

What is the job about?

As a Drug Safety Advisor, you focus on providing high-quality, comprehensive, technical and scientific information services to our customers regarding their product range. This involves supporting and enhancing the safe and effective use of products, enabling our customers to make informed decisions about their product range.

• You provide a first-line technical and scientific information service to the internal pharmacovigilance (PV) team and customers;
• You handle all medical enquiries, in particular, adverse event reports and pregnancy reports, in line with procedures;
• You take care of a medical evaluation of spontaneous adverse events;
• You contribute to and perform medical assessments of the specific documents (e.g. safety profile of medicines, detected scientific literature, signals, cases etc.; Periodic and Development Safety reports, Risk Management Plans, DHPC etc.);
• You report PSUR/DSUR/ASR/RMP/cases to relevant Authorities within defined time frames and ensure appropriate levels of follow-up with reporters to fulfil all legal and regulatory requirements;
• You ensure all appropriate reports are distributed to regulatory authorities, Ethics Committees and investigators within regulated timeframes;
• You provide pharmacovigilance expertise to Risk Management planning cross-functional teams with input to formulation, implementation, maintenance and tracking of local RMPs;
• You provide a comprehensive information service to external healthcare professionals and patients on the safety of company products in the scope of Risk Minimization Measures.

What do we expect from you?

• You have a Master’s degree in science;
• You have a minimum of 3 years of experience as a Medical Advisor/ Drug Safety Advisor;
• You have a strong knowledge of PV processes and European PV legislation;
• You have a minimum level of C2 in English, the knowledge of another EU language is a plus;
• You can work in a fast-moving working environment;
• You are stress-resistant, work autonomously and flexible;
• You are quality-oriented and meticulous in figuring out and formatting your work;
• You are result-oriented.

What do we offer?

• Working at Qplus consult means every day brings new challenges and opportunities.
• You will be part of a dynamic, fast-growing company with a global customer base.
• Our workplace fosters a healthy environment with fresh fruit, sit-stands desks or desk bikes/treadmills;
• Attractive and competitive basic salary;
• Additional benefits like insurances, meal vouchers, eco vouchers, and company car with fuel card;
• Training and career growth opportunities.

Who are we?

With our 6 service lines (Medical Affairs, Pharmacovigilance, Quality Management, Regulatory Affairs, Auditing and Training), we are an expert in our job within the pharmaceutical industry.

We emphasise our values: client first, dedication, loyalty, passion, professionalism and performance.

Our main focus is to build a long-term relationship with each of our clients to provide a service of excellence in a timely and cost-efficient manner. To meet these expectations, we have a team of professional experts who are exceptionally highly trained and ready to provide excellent service every day.

Watch our video and join us at Qplus consult! https://bit.ly/40igh7h